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Mass spectrometry imaging (MSI) or imaging mass spectrometry (IMS) is a technique used in mass spectrometry to visualize the spatial distribution of chemical compositions e.g. compounds, biomarkers, metabolites, peptides or proteins by their molecular masses. Although widely used traditional methodologies like radiochemistry and immunohistochemistry achieve the same goal as MSI, they are limited in their abilities to analyze multiple samples at once, and can prove to be lacking if researchers do not have prior knowledge of the samples being studied. Most common ionization technologies in the field of MSI are DESI imaging, MALDI imaging and secondary ion mass spectrometry imaging (SIMS imaging).

History

More than 50 years ago, IMS was introduced using secondary ion mass spectrometry (SIMS). However, it was the pioneering work of Richard Caprioli and colleagues in the late 1990s, demostrating how matriz-assisted laser desorption/ionization (MALDI) could be applied to visualize large biomolecules (as proteins and lipids) in cells and tissue to reveal the function of these molecules and how function is changed by diseases like cancer, which led to the widespread use of IMS. Nowadays, different ionization techniques have been used, including SIMS, MALDI and desorption electrospray ionization (DESI), as well as other technologies. Still, MALDI is the current dominant technology with regard to clinical and biological applications of MSI.

Operation Principle

The MSI is based on the spatial distribution of the sample. Therefore, the operation principle depends on the technique that is used to obtain the spatial information. The two techniques used in MSI are: microprobe and microscope.

Microprobe

This technique is performed using a focused ionization beam to analyze a specific region of the sample by generating a mass spectrum. The mass spectrum is stored along with the spatial coordination where the measurement took place. Then, a new region is selected and analyzed by moving the sample or the ionization beam. This steps are repeated until the entire sample has been scanned. By coupling all individual mass spectra, a distribution map of intensities as a function of x and y locations can be plotted. As a result reconstructed molecular images of the sample are obtained.

Microscope

In this technique, a 2D position-sensitive detector is used to measure the spatial origin of the ions generated at the sample surface by the ion optics of the instruments. The resolution of the spatial information will depend on the magnification of the microscope, the quality of the ions optics and the sensitivity of the detector. A new region still need to be scanned. but the number of positions drastically reduces. The limitation of this mode is the finite depth of vision present with all microscopes.

Most of the information below is related with the microprobe technique, since this method is the most simple and common used for MSI.

Ion Source Dependence

The Ionization techniques available for IMS are suited to different applications. Some of the criteria for choosing the ionization method are the sample preparation requirement and the parameters of the measurement, as resolution, mass range and sensitivity. Based on that, the most common used ionization method are MALDI, SIMS AND DESI which are described below. Still, other minor techniques used are laser ablation electrospray ionization (LAESI) and laser-ablation-inductively coupled plasma (LA-ICP).

SIMS imaging

Secondary ion mass spectrometry (SIMS) is used to analyze solid surfaces and thin films by sputtering the surface with a focused primary ion beam and collecting and analyzing ejected secondary ions. There are many different sources for a primary ion beam. However, the primary ion beam must contain ions that are at the higher end of the energy scale. Some common sources are: Cs⁺, O₂⁺, O, Ar⁺ and Ga⁺. SIMS imaging is performed in a manner similar to electron microscopy; the primary ion beam is emitted across the sample while secondary mass spectra are recorded. SIMS proves to be advantageous in providing the highest image resolution but only over small area of samples. More, this technique is widely regarded as one of the most sensitive forms of mass spectrometry as it can detect elements as small as 10⁻⁶-10⁻⁹.

Multiplexed ion beam imaging (MIBI) is a SIMS method that uses metal isotope labeled antibodies to label compounds in biological samples.

Developments within SIMS: Some chemical modifications have been made within SIMS to increase the efficiency of the process. There are currently two separate techniques being used to help increase the overall efficiency by increasing the sensitivity of SIMS measurements: matrix-enhanced SIMS (ME-SIMS) - This has the same sample preparation as MALDI does as this simulates the chemical ionization properties of MALDI. ME-SIMS does not sample nearly as much material. However, if the analyte being tested has a low mass value then it can produce a similar looking spectra to that of a MALDI spectra. ME-SIMS has been so effective that it has been able to detect low mass chemicals at sub cellular levels that was not possible prior to the development of the ME-SIMS technique. The second technique being used is called sample metallization (Meta-SIMS) - This is the process of gold or silver addition to the sample. This forms a layer of gold or silver around the sample and it is normally no more than 1-3 nm thick. Using this technique has resulted in an increase of sensitivity for larger mass samples. The addition of the metallic layer also allows for the conversion of insulating samples to conducting samples, thus charge compensation within SIMS experiments is no longer required.

MALDI imaging

Mouse kidney: (a) MALDI spectra from the tissue. (b) H&E stained tissue. N-glycans at m/z = 1996.7 (c) is located in the cortex and medulla while m/z = 2158.7 (d) is in the cortex, (e) An overlay image of these two masses, (f) untreated control tissue.

Main article: MALDI imaging

Matrix-assisted laser desorption ionization can be used as a mass spectrometry imaging technique for relatively large molecules. It has recently been shown that the most effective type of matrix to use is an ionic matrix for MALDI imaging of tissue. In this version of the technique the sample, typically a thin tissue section, is moved in two dimensions while the mass spectrum is recorded. Although MALDI has the benefit of being able to record the spatial distribution of larger molecules, it comes at the cost of lower resolution than the SIMS technique. The limit for the lateral resolution for most of the modern instruments using MALDI is 20 $\mu$m. MALDI experiments commonly use either an Nd:YAG (355 nm) or N₂ (337 nm) laser for ionization.

Pharmacodynamics and toxicodynamics in tissue have been studied by MALDI imaging.

DESI imaging

Desorption electrospray Ionization is a less destructive technique, which couples simplicity and rapid analysis of the sample. The sample is sprayed with an electrically charged solvent mist at an angle that causes the ionization and desorption of various molecular species. Then, two-dimensional maps of the abundance of the selected ions in the surface of the sample in relation with the spatial distribution are generated. This technique is applicable to solid, liquid, frozen and gaseous samples. Moreover, DESI allows analyzing a wide range of organic and biological compounds, as animal and plant tissues and cell culture samples, without complex sample preparation Although, this technique has the poorest resolution among other, it can create high-quality image from a large area scan, as a whole body section scanning.

Comparative between the Ionization Techniques

Comparison of typical parameters among IMS techniques

	Ionization Source	Type of Ionization	Analytes	Spatial Resolution	Mass Range
SIMS	Ion gun	Hard	Elemental ions, small molecules, lipids	<10 $\mu$m	0-1000 Da
MALDI	UV laser beam	Soft	Lipids, peptide, proteins	20 $\mu$m	0-100 000 Da
DESI	Solvent Spray	Soft	Small molecules, lipids, peptides	100 $\mu$m	0-2000 Da

Combination of Various IMS Techniques and other imaging techniques

Combining various IMS techniques can be beneficial, since each particular technique has its own advantage. For example, when information regards both proteins and lipids are necessary in the same tissue section, performing DESI to analyze the lipid, followed by MALDI to obtain information about the peptide, and finalize applying a stain (haematoxylin and eosin) for medical diagnosis of the structural characteristic, of the tissue. Among IMS with other imaging techniques, IMS with fluorescence staining and IMS with magnetic resonance imaging (MRI) can be highlighted. Fluorescence staining can give information of the appearance of some proteins present in any process inside a tissue, while IMS may give information about the molecular changes presented in that process. Combining both techniques, multimodal picture or even 3D images of the distribution of different molecules can be generated. In contrast, MRI with IMS combines the continuous 3D representation of MRI image with detailed structural representation using molecular information from IMS. Even though, IMS itself can generate 3D images, the picture is just part of the reality due to the depth limitation in the analysis, while MRI provides, for example, detailed organ shape with additional anatomical information. This coupled technique can be beneficial for cancer precise diagnosis and neurosurgery.

Data Processing

Standard data format for mass spectrometry imaging datasets

An useful data format for IMS is imML data format, because several imaging MS software tools support it. The advantage of this format is the flexibility to exchange data between different instruments and data analysis softwares. All necessary information for evaluating and implementing imzML can be found at http://www.imzML.org.

Software

There are many free software packages available for visualization and mining of imaging mass spectrometry data. Converters from Thermo Fisher format, Analyze format, GRD format and Bruker format to imzML format were developed by the Computis project. Some software modules are also available for viewing mass spectrometry images in imzML format: Biomap] (Novartis, free), Datacube Explorer (AMOLF, free), EasyMSI (CEA), Mirion (JLU), MSiReader (NCSU, free) and SpectralAnalysis.

For processing .imzML files with the free statistical and graphics language R, a collection of R scripts is available, which permits parallel-processing of large files on a local computer, a remote cluster or on the Amazon cloud.

Another free statistical package for processing imzML and Analyze 7.5 data in R exists, Cardinal .

Applications

A remarkable ability of IMS is to find out the localization of biomolecules in tissues, even though there are no previous information about them. This feature has made IMS an unique tool for clinical research and pharmacological research. It provides information about biomolecular changes related with diseases by tracking proteins, lipids, and cell metabolism. For example, identifying biomakers by IMS can show detailed cancer diagnosis. In addition, low cost imaging for pharmaceuticals studies can be acquired, such as images of molecular signatures that would be indicative of treatment response for a specific drug.

Advantages, Challenges and Limitations

The main advantage of MSI for studying the molecules location and distribution within the tissue is that this analysis can provide either greater selectivity, more information or more accuracy. Moreover, this tool requires less investment of time and resources for similar results.

Current Complexity for MSI

Difficult/Why?	Readily Performed
Proteomics: mass range limited	Drug and metabolite
Free drug from total: Does break interactions	On-tissue quantification
Terminal sampling required: no monitoring	Pathology support
Sub-cellular: instrument limitations	Studying unantecipated outcomes
Clinical samples: sample collection	Biomarkers analysis
Antibodies	Comparing tissues for unkown
	Blood brain barriers/tumours